CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 57 enrolled
Drug / intervention
Cytosorb therapydevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04913298
NCT04913298N/ACompleted

Prospective Quality Assurance Study for the Application of Cytosorb® in Patients With Cytokine Storm, Rhabdomyolysis and Acute Liver Failure

Ludwig-Maximilians - University of Munich·interventional·Posted Jun 4, 2021·Updated Feb 22, 2024

In Brief

A clinical study evaluating Cytosorb therapy for Rhabdomyolysis and 2 related conditions. Completed, enrolled 57 participants across 1 site.

Detailed Summary

The mortality of critically ill patients is persistently high and requires targeted therapy of pathophysiological disorders. One approach to optimize therapy is the use of the cytokine adsorber Cytosorb®, which has a CE certification for the indications hyperinflammation, rhabdomyolysis and liver failure and is therefore frequently used in patients with sepsis, polytrauma and acute liver failure. Although few clinical data describe the efficiency mostly retrospectively, there are no data on real-time elimination performance and saturation kinetics during the course of treatment. These questions should be answered by the present study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesGermany
Collaborators--

Timeline

N/ACompletedFinished
20222023202420252026
First PostedJun 4, 2021
Enrollment StartMar 1, 2021
Primary CompletionApr 30, 2023
Study CompletionDec 15, 2023
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 5.1 years ago

Interventions

Cytosorb therapydevice

Start of Cytosorb therapy is at the discretion of the attending physician